Reconfigurable DNA origami hinges for nanopore detection of microRNA

The advancement of biosensor technology is driving the development of ultra sensitive detection methods, with single-molecule sensing emerging as a particularly promising approach. Nanopore sensing enables the detection of biomarker sat the single-molecule level, offering high sensitivity and specificity for biological sample analysis. In this study, we designed a reconfigurable DNA origami hinge as a molecular carrier for nanopore-based detection of miRNA-141-3p, a biomarker associated with prostate cancer. The hinge undergoes a controlled transition from a closed to an extended state upon binding to miRNA-141-3p, with distinct ionic current signatures recorded before and after reconfiguration during nanopore translocation experiments. Our approach demonstrates detection sensitivity down to the nanomolar level and exhibits excellent selectivity, effectively distinguishing miRNA-141-3p from closely related sequences. These findings highlight the potential of DNA nanostructure-based nanopore sensing for ultrasensitive and selective biomarker detection in biological samples.

Publication Details

Journal
Apollo (University of Cambridge)
Published
2025-05-21
DOI
https://doi.org/10.17863/cam.118349
Primary Topic
Gaze Tracking and Assistive Technology
Type
article
Field-Weighted Citation Impact
0.00

Funders

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article

Reconfigurable DNA origami hinges for nanopore detection of microRNA

Apollo (University of Cambridge)
Gaze Tracking and Assistive Technology
article

Reconfigurable DNA origami hinges for nanopore detection of microRNA

article en

Abstract

The advancement of biosensor technology is driving the development of ultra sensitive detection methods, with single-molecule sensing emerging as a particularly promising approach. Nanopore sensing enables the detection of biomarker sat the single-molecule level, offering high sensitivity and specificity for biological sample analysis. In this study, we designed a reconfigurable DNA origami hinge as a molecular carrier for nanopore-based detection of miRNA-141-3p, a biomarker associated with prostate cancer. The hinge undergoes a controlled transition from a closed to an extended state upon binding to miRNA-141-3p, with distinct ionic current signatures recorded before and after reconfiguration during nanopore translocation experiments. Our approach demonstrates detection sensitivity down to the nanomolar level and exhibits excellent selectivity, effectively distinguishing miRNA-141-3p from closely related sequences. These findings highlight the potential of DNA nanostructure-based nanopore sensing for ultrasensitive and selective biomarker detection in biological samples.

Apollo (University of Cambridge)
European Commission, Engineering and Physical Sciences Research Council, Biotechnology and Biological Sciences Research Council
Openalex Percentile: Top 54%
Gaze Tracking and Assistive Technology
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Reconfigurable DNA origami hinges for nanopore detection of microRNA · Apollo (University of Cambridge) (2025) | TGRS Research Map | TGRS